Short somatic alterations at the site of copy number variation in breast cancer

Copy number variation (CNV) is a polymorphism in the human genome involving DNA fragments larger than 1 kb. Copy number variation sites provide hotspots of somatic alterations in cancers. Herein, we examined somatic alterations at sites of CNV in DNA from 20 invasive breast cancers using a Comparati...

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Detalles Bibliográficos
Autores principales: Murakami, Fumi, Tsuboi, Yumi, Takahashi, Yuka, Horimoto, Yoshiya, Mogushi, Kaoru, Ito, Takeshi, Emi, Mitsuru, Matsubara, Daisuke, Shibata, Tatsuhiro, Saito, Mitsue, Murakami, Yoshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Genetics, Genomics, and Proteomics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780029/
https://www.ncbi.nlm.nih.gov/pubmed/32860329
http://dx.doi.org/10.1111/cas.14630

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780029/
https://www.ncbi.nlm.nih.gov/pubmed/32860329
http://dx.doi.org/10.1111/cas.14630

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